Silke B, Verma S P, Hafizullah M, Reynolds G, Frais M A, Jackson N C, Taylor S H
Postgrad Med J. 1984;60 Suppl 4:29-34.
The haemodynamic dose-response effects of the slow-calcium channel blocker nicardipine were evaluated in fifteen male patients with uncomplicated acute myocardial infarction. Following a 1 hr control period, during which the stability of base-line control haemodynamic variables was confirmed, four i.v. boluses of 1.25, 1.25, 2.5 and 5.0 mg of the drug (cumulative dosage 1.25, 2.5, 5.0 and 10.0 mg) were administered at 15 min intervals. The plasma concentrations achieved are within the previously described therapeutic range (greater than 20 micrograms/l). Nicardipine resulted in linear reductions in systemic arterial pressure and vascular resistance, and dose-related increases in heart rate, cardiac and stroke output without change in the left heart filling pressure. Intravenous nicardipine did not induce any depression of left ventricular pumping performance in our patients in the early stages of uncomplicated myocardial infarction.
在15例无并发症的急性心肌梗死男性患者中评估了慢钙通道阻滞剂尼卡地平的血流动力学剂量反应效应。在1小时的对照期后,在此期间确认了基线对照血流动力学变量的稳定性,以15分钟的间隔静脉注射4次剂量分别为1.25、1.25、2.5和5.0毫克的该药物(累积剂量为1.25、2.5、5.0和10.0毫克)。所达到的血浆浓度在先前描述的治疗范围内(大于20微克/升)。尼卡地平导致体循环动脉压和血管阻力呈线性降低,心率、心输出量和每搏输出量与剂量相关增加,而左心充盈压无变化。在无并发症心肌梗死早期阶段,静脉注射尼卡地平未引起我们患者左心室泵血功能的任何抑制。